FDAFDA · Food and drugs·Recall number D-0866-2016
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.
Published June 1, 2016 · Recall initiated: May 4, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impuities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Fresenius Kabi USA, LLC
- Distributor
- Nationwide and Puerto Rico.
- Lot
- Lot # 6108322; Exp. 04/16 Lot # 6108824; Exp. 07/16
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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